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Species-Conserved SYNGAP1 Phenotypes Associated with Neurodevelopmental Disorders

SYNGAP1 loss-of-function variants are causally associated with intellectual disability, severe epilepsy, autism spectrum disorder and schizophrenia. While there are hundreds of genetic risk factors for neurodevelopmental disorders (NDDs), this gene is somewhat unique because of the frequency and pen...

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Detalhes bibliográficos
Publicado no:Mol Cell Neurosci
Main Authors: Kilinc, Murat, Creson, Thomas, Rojas, Camilo, Aceti, Massimiliano, Ellegood, Jacob, Vaissiere, Thomas, Lerch, Jason P., Rumbaugh, Gavin
Formato: Artigo
Idioma:Inglês
Publicado em: 2018
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6128754/
https://ncbi.nlm.nih.gov/pubmed/29580901
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mcn.2018.03.008
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